Meta description (140–160): NANOTEC’s Nanoparticles Production Service turns nano-enabled concepts into real, testable ingredients, from trial batches to scale-up under ASEAN GMP Cosmetic–aligned workflows with coordinated QC and stability support.

SEO keywords: nanoparticles production, nanotec, nanotechnology, nano actives manufacturing, nanotechnology Thailand, ASEAN GMP cosmetic, nano ingredients scale up, trial production nanocarriers, cosmetic raw materials nano, stability testing nano, microbiological testing nano, process optimization nanotech

The Nanoparticles and Cosmetics Production Plant operated by the National Nanotechnology Center (NANOTEC, NSTDA) helps companies move from idea to evidence with end-to-end nanoparticle production. Whether you are screening a new nano-active, preparing for a market trial, or getting ready for industrial supply, our team delivers trial batches, process optimization, and scale-up with the documentation you need for internal QA and partner review.

When your intended use is within cosmetics, we align production practices and documentation with ASEAN GMP Cosmetic expectations to smooth downstream manufacturing and acceptance. In the same facility, you can also coordinate physical, microbiological, and stability tests so material, data, and timelines stay synchronized.

Starting price: Trial-scale Nanoparticles Production from THB 34,500 per batch (formal quotation follows scoping).

Why Use a Dedicated Nanoparticle Production Service?

• De-risk development. Trial batches reveal real behavior, stability, handling, and compatibility, before you commit to large volumes.
• Shorten the loop. Production and testing can be coordinated together, reducing handoffs and delays.
• Build a defensible record. You receive clearly organized QC and (optionally) stability data to support decisions, partner discussions, and product files.
• Scale with confidence. Once a process window is defined, we help you move to larger runs using the same disciplined approach.

What We Produce

We manufacture nanoparticle-based active ingredients and nano-enabled raw materials to be used downstream (e.g., in cosmetic formulations). Because client needs vary, composition and process are finalized during scoping. Typical outputs include:

• Nano-actives / nano-enabled ingredients designed to improve solubility, stability, delivery, or sensory profile of your functional compounds.
• Trial-scale batches for laboratory evaluation, panel testing, or market trials.
• Pilot or larger runs (quoted separately) when you are ready to progress toward commercial supply.
• Supporting documentation from concise QC summaries to stability plans so your team can assess performance and risk quickly.

If you need finished-product runs as well, you can pair this service with Cosmetics Trial Production and Cosmetics Commercial Production (handled as separate engagements).

How We Work: Step-by-Step

1) Discovery & Scoping

You share your objectives (e.g., target actives, intended use, desired batch size, constraints such as solvents to avoid). We propose a trial-production plan, a QC/stability panel sized to your decision needs, and a quotation. When the output is destined for cosmetics, we map the workflow to ASEAN GMP Cosmetic–aligned practices.

2) Trial Production (from THB 34,500 per batch)

We manufacture a trial batch to verify feasibility and capture real process data. You can request iterative trials to fine-tune composition or parameters. QC at this stage typically includes key physicochemical checks and a basic microbiological screen (panel tailored in scoping).

3) Process Optimization & Scale-Up Readiness

Using trial data, we set critical parameters and in-process controls that drive consistency. We also agree on the release tests that make sense for your risk level and end use.

4) Pilot / Commercial Production (optional)

When you are ready, we schedule larger runs and compile batch documentation aligned to your downstream QA. For cosmetic applications, the flow remains ASEAN GMP Cosmetic–aligned.

5) Evidence & Post-Batch Support

As requested, we coordinate physical, microbiological, and stability testing. You receive interpretable summaries clear enough for non-specialists yet structured for QA.

What You Receive (Typical Deliverables)

• Manufactured material in the agreed format (e.g., dispersion or concentrate), labeled for traceability.
• Certificate/Summary of Analysis listing release tests, methods, and acceptance criteria agreed at scoping.
• Production summary describing the high-level process map and key controls for the lot (suitable for internal review and supplier qualification workflows).
• Stability plan & interim data (if contracted) to help estimate shelf life and define storage statements.
• Handling & storage guidance derived from batch behavior and early stability observations.

Quality & Compliance

• ASEAN GMP Cosmetic–aligned practices when the nanoparticle output is intended for cosmetic manufacturing.
• Integrated testing (physical, microbiological, stability) available in the same ecosystem to reduce transfer risks.
• Traceability & documentation that support audits, partner reviews, and downstream manufacturing.

Pricing & Options

• Trial-scale Nanoparticles Production:from THB 34,500 per batch
  Optional add-ons (quoted separately):
  • Additional iterative trials
  • Expanded physicochemical or microbiological QC
  • Stability studies (protocol design, execution, reporting)
  • Pilot or commercial runs with enhanced documentation
  • Scheduling with Cosmetics Trial or Cosmetics Commercial Production

We will right-size the package for your goal: screening a concept, seeding a market test, preparing investor demos, or locking a process for full-scale supply.

Frequently Asked Questions

What is covered in the starting price?
The entry price covers one trial-scale batch produced under the agreed plan plus a basic QC panel suitable for early technical validation. Expanded testing and iterative trials are optional.

Can you work from a performance brief instead of a recipe?
Yes. If you know what you want the material to do (e.g., improve stability of a particular active), we can propose a feasibility-first trial that balances cost and time.

Do you test safety or efficacy?
For ingredients intended for cosmetics, we can coordinate physical, microbiological, and stability studies that inform shelf life and handling. If you require safety or toxicology testing for finished products, see our Safety & Toxicology Testing Services (e.g., in-vitro cytotoxicity and in-vitro micronucleus per OECD 487).

Will you help with shelf-life statements?
Yes. We design and execute stability studies with defined conditions and checkpoints. Reports summarize observations in a decision-ready format you can use with partners and QA.

How do you handle confidentiality?
Client information, formulations, and data are treated as confidential. We can countersign your NDA during scoping.

Who This Service Is For

• Brands & startups validating nano-enabled actives with real batches for panel or market tests.
• OEM/ODM manufacturers requiring locally produced nano-ingredients with traceability and GMP-aligned documentation.
• R&D and formulation teams translating lab concepts to scalable processes with clear specifications.
• Distributors of cosmetic raw materials seeking Thai-made nano-actives supported by QC/stability evidence.

Suggested Internal Links

• Cosmetics Trial Production – pilot runs of finished formulations that incorporate your nano-ingredient.
• Cosmetics Commercial Production – industrial-scale batches aligned with ASEAN GMP Cosmetic.
• Safety & Toxicology Testing – e.g., in-vitro cytotoxicity and in-vitro micronucleus (OECD 487).
• Thermal & Stability Testing Hub – design and execution of stability programs.

Contact Us

National Nanotechnology Center (NANOTEC)
Infrastructure Services
143 INC 2 (B), Thailand Science Park, Phahonyothin Road,
Khlong Nueng, Khlong Luang, Pathum Thani 12120, Thailand
Tel. +66 2 564 7100 ext. 6517, 6625, 6680
Email: bdis-infs@nanotec.or.th

Ready to scope your first batch?Share your target active(s), intended use, and desired batch size. We’ll return a practical trial plan and a transparent quotation, so you can move from concept to evidence with confidence.